ArticleFrontiers in cell and developmental biology2025
Osteoprogenitor cells from non-regenerative bone show greater resistance to cellular stress than those from regenerative bone.
Article in Frontiers in cell and developmental biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Introduction: Bone regeneration following injury depends on osteoprogenitor cells derived predominantly from the periosteum. Incomplete regeneration has been attributed to both cell-extrinsic factors (e.g., environment, inflammation, mechanical instability) and cell-intrinsic factors (e.g., impaired proliferation or differentiation of stem cells). In the digit amputation mouse model, amputation through the third phalanx (P3) supports complete regeneration, while amputation through the second phalanx (P2) results in callus formation and scarring. Periosteal cells are known to be the major contributing cell source for repair and regeneration. Yet the healing outcomes of P2 and P3 amputations are significantly different. This study tests whether P2 and P3 cells are functionally equivalent. Methods and results: Using Discussion: Together, these findings suggest that periosteal cells exhibit intrinsic differences based on anatomical location, which may influence their regenerative capacity and contribute to different healing outcomes.
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